FDA 510(k) Unknown 🇺🇸 United States

SUGITA ANEURYSM CLIPS, APPLIERS & CASE

K Number: K791978 · Decision Sep 28, 1979
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
152
Review Days

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Basic Information

Device Name
SUGITA ANEURYSM CLIPS, APPLIERS & CASE
K Number
K791978
Clearance Type
Traditional
Decision
Unknown
Applicant
Codman & Shurtleff, Inc.
Date Received
September 28, 1979
Decision Date
September 28, 1979
Advisory Committee
Unknown
Review Advisory Committee
NE
Third Party
N

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